FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SHILEY ARTERIAL FILTER

K Number: K811379 · Decision Jun 9, 1981
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
94
Applicant Total
174
Review Days
25

Basic Information

Device Name
SHILEY ARTERIAL FILTER
K Number
K811379
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4260
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
SHILEY, INC.
Date Received
May 15, 1981
Decision Date
June 9, 1981
Product Code
DTM
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line

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